Q79.69
BillableOther Ehlers-Danlos syndromes
Other Ehlers-Danlos syndromes
Status
Billable / Specific
Parent Code
Q79.6Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Ehlers-Danlos syndrome type 6A25606004
- Ehlers-Danlos syndrome, hydroxylysine-deficient25606004
- Ehlers-Danlos syndrome, lysyl hydroxylase deficient25606004
- Hydroxylysine-deficient collagen disease25606004
- Ocular scoliotic EDS (Ehlers-Danlos syndrome)25606004
- Protocollagen lysyl hydroxylase deficiency25606004
- Ehlers-Danlos syndrome type 850869007
- Ehlers-Danlos syndrome type VIII50869007
- Ehlers-Danlos syndrome, periodontitis type50869007
- Ehlers-Danlos syndrome, type 850869007
- Periodontal Ehlers-Danlos syndrome50869007
- Periodontitis associated with Ehlers-Danlos syndrome type VIII50869007
- Arthrochalasia Ehlers-Danlos syndrome55711009
- Arthrochalasia multiplex congenita55711009
- Arthrochalasis multiplex congenita55711009
- Ehlers-Danlos syndrome type 755711009
- Cutis laxa, x-linked59399004
- Ehlers-Danlos syndrome type 9 X-linked59399004
- Ehlers-Danlos syndrome, mental retardation type59399004
- Ehlers-Danlos syndrome, occipital horn type59399004
- Ehlers-Danlos syndrome, type 959399004
- Ehlers-Danlos syndrome, x-linked skeletal type59399004
- Occipital horn syndrome59399004
- Ehlers-Danlos syndrome type V67202007
- Ehlers-Danlos syndrome, type 567202007
- X-linked Ehlers-Danlos syndrome67202007
- Congenital humpback71311003
- Congenital hunchback71311003
- Congenital kyphosis71311003
- Ehlers-Danlos syndrome type XI71322004
- Ehlers-Danlos syndrome, familial joint laxity type71322004
- Ehlers-Danlos syndrome, type 1171322004
- Familial articular hypermobility syndrome71322004
- Familial generalised articular hypermobility71322004
- Familial generalized articular hypermobility71322004
- Familial joint instability syndrome71322004
- Familial joint laxity71322004
- Copper metabolism disorder79886009
- Disorder of copper metabolism79886009
- Ehlers-Danlos syndrome with platelet dysfunction83586000
- Ehlers-Danlos syndrome, dysfibronectinaemic83586000
- Ehlers-Danlos syndrome, dysfibronectinemic83586000
- Ehlers-Danlos syndrome, type 1083586000
- Congenital kyphoscoliosis405772002
- Corneal thinning423459005
- Thin cornea423459005
- Periodontitis associated with genetic disorder710903001
- Periodontitis co-occurrent with genetic disorder710903001
- Ehlers-Danlos syndrome kyphoscoliotic type718211004
- Ehlers-Danlos syndrome type 6718211004
- Ehlers-Danlos syndrome type VI718211004
- Brittle cornea syndrome719096006
- Ehlers-Danlos syndrome type 6B719096006
- Ehlers-Danlos syndrome cardiac valvular type720858001
- Ehlers-Danlos syndrome kyphoscoliotic and deafness type720859009
- Ehlers-Danlos syndrome kyphoscoliotic and hearing loss type720859009
- Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and deafness720859009
- Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency720859009
- Adducted thumbs, arthrogryposis syndrome, Dundar type720860004
- Ehlers-Danlos syndrome Kosho type720860004
- Ehlers-Danlos syndrome arthrogryposic type720860004
- Ehlers-Danlos syndrome musculocontractural type720860004
- B4GALT7-related spondylodysplastic EDS (Ehlers-Danlos syndrome)720861000
- Defective biosynthesis of proteodermatan sulfate720861000
- Defective biosynthesis of proteodermatan sulphate720861000
- Ehlers-Danlos syndrome progeroid type720861000
- Galactosyltransferase I deficiency720861000
- Xylosylprotein 4-beta-galactosyltransferase deficiency720861000
- Ehlers-Danlos syndrome spondylocheirodysplastic type773276004
- SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome773276004
- Spondylocheirodysplastic Ehlers-Danlos syndrome773276004
- Classical-like Ehlers-Danlos syndrome type 1778022009
- Ehlers-Danlos syndrome classic-like type778022009
- Ehlers-Danlos syndrome due to tenascin-X deficiency778022009
- Dermatosparaxis EDS (Ehlers-Danlos syndrome)1237225007
- Dermatosparaxis Ehlers-Danlos syndrome1237225007
- Ehlers-Danlos syndrome type 7C1237225007
- Human dermatosparaxis EDS VIIC (Ehlers-Danlos syndrome type 7C)1237225007
- Spondylodysplastic Ehlers-Danlos syndrome1251488008
- B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome1251499005
- Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome1251499005
- Ehlers-Danlos syndrome progeroid type 21251499005
- Ehlers-Danlos myopathy overlap syndrome1255116001
- Myopathic EDS (Ehlers-Danlos syndrome)1255116001
- Myopathic Ehlers-Danlos syndrome1255116001
- AEBP1-related EDS (Ehlers-Danlos syndrome)1255121003
- AEBP1-related Ehlers-Danlos syndrome1255121003
- Classical-like Ehlers-Danlos syndrome type 21255121003
Frequently Asked Questions
What is the ICD-10 code for other ehlers-danlos syndromes?
The ICD-10-CM code for other ehlers-danlos syndromes is Q79.69. The full clinical description is "Other Ehlers-Danlos syndromes". Q79.69 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q79.69 mean?
ICD-10-CM code Q79.69 represents "Other Ehlers-Danlos syndromes". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q79.69 a billable code?
Yes, Q79.69 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q79.69 in?
Q79.69 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q79.69 map to?
Q79.69 maps to 25 SNOMED CT concepts: 1255121003, 720860004, 55711009, 1251499005, 720861000, and 20 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q79.69?
Q79.69 is linked to 1 UMLS Concept Unique Identifier: C5140892. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.